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Structure−Property Relationships of Stable Free Radicals: Verdazyls with Electron-Rich Aryl Substituents

Journal of organic chemistry, 2009-03, Vol.74 (5), p.1850-1857

2009

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Geometric Control of Ground State Multiplicity in a Copper(I) Bis(verdazyl) Complex

Inorganic chemistry, 2010-09, Vol.49 (18), p.8573-8577

2010

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Modifications of Tanabe-Sugano d6 Diagram Induced by Radical Ligand Field: Ab Initio Inspection of a Fe(II)-Verdazyl Molecular Complex

Inorganic chemistry, 2023-04, Vol.62 (14), p.5737-5743

2023

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Modifications of Tanabe-Sugano d 6 Diagram Induced by Radical Ligand Field: Ab Initio Inspection of a Fe(II)-Verdazyl Molecular Complex

Inorganic chemistry, 2023-04, Vol.62 (14), p.5737-5743

2023

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Recent advances in congenital heart disease genomics

F1000 research, 2017, Vol.6, p.869-869

2017

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Strong ferromagnetic metal-ligand exchange in a nickel bis(3,5-dipyridylverdazyl) complex

Chemical communications (Cambridge, England), 2010-09, Vol.46 (35), p.6590-6592

2010

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Combined Mutation Screening of NKX2-5, GATA4, and TBX5 in Congenital Heart Disease: Multiple Heterozygosity and Novel Mutations

Congenital heart disease, 2012-03, Vol.7 (2), p.151-159

2012

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Body composition and clinical outcome measures in patients with myotonic dystrophy type 1

Neuromuscular disorders : NMD, 2017-03, Vol.27 (3), p.286-289

2017

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Radical−Radical Interaction through a Saturated Link: Methylenebis-6-oxoverdazyl

Journal of organic chemistry, 2006-06, Vol.71 (13), p.4889-4895

2006

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Coordinated Hydrazone Ligands as Nucleophiles: Reactions of Fe(papy)2

Inorganic chemistry, 2004-12, Vol.43 (26), p.8355-8360

2004

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Effect of deletion of the protein kinase PRKD1 on development of the mouse embryonic heart

Journal of anatomy, 2024-07, Vol.245 (1), p.70-83

2024

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Acetylation of TBX5 by KAT2B and KAT2A regulates heart and limb development

Journal of molecular and cellular cardiology, 2018-01, Vol.114, p.185-198

2018

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HDAC4 and 5 repression of TBX5 is relieved by protein kinase D1

Scientific reports, 2019-11, Vol.9 (1), p.17992-10, Article 17992

2019

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Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans

American journal of human genetics, 2014-04, Vol.94 (4), p.574-585

2014

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Zebrafish deficient for Muscleblind-like 2 exhibit features of myotonic dystrophy

Disease models & mechanisms, 2011-05, Vol.4 (3), p.381-392

2011

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Flies deficient in Muscleblind protein model features of myotonic dystrophy with altered splice forms of Z-band associated transcripts

Human genetics, 2006-11, Vol.120 (4), p.487-499

2006

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Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16

Nature genetics, 2013-07, Vol.45 (7), p.822-824

2013

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Coordination Chemistry of Verdazyl Radicals

Comments on modern chemistry. Part A, Comments on inorganic chemistry, 2015-01, Vol.35 (1), p.1-17

Brook, David J. R.

2015

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Tropomyosin 1: Multiple roles in the developing heart and in the formation of congenital heart defects

Journal of molecular and cellular cardiology, 2017-05, Vol.106, p.1-13

2017

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High-content screening identifies small molecules that remove nuclear foci, affect MBNL distribution and CELF1 protein levels via a PKC-independent pathway in myotonic dystrophy cell lines

Human molecular genetics, 2014-03, Vol.23 (6), p.1551-1562

2014

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Verdazyl-ribose: A new radical for solid-state dynamic nuclear polarization at high magnetic field

Journal of magnetic resonance (1997), 2018-04, Vol.289, p.122-131

2018

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Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation

PloS one, 2009-03, Vol.4 (3), p.e4978-e4978

2009

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Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

Nature (London), 1992-02, Vol.355 (6360), p.545-546

1992

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Structure−Property Relationships of Stable Free Radicals: Verdazyls with Electron-Rich Aryl Substituents

Geometric Control of Ground State Multiplicity in a Copper(I) Bis(verdazyl) Complex

Modifications of Tanabe-Sugano d6 Diagram Induced by Radical Ligand Field: Ab Initio Inspection of a Fe(II)-Verdazyl Molecular Complex

Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot

Modifications of Tanabe-Sugano d 6 Diagram Induced by Radical Ligand Field: Ab Initio Inspection of a Fe(II)-Verdazyl Molecular Complex

Recent advances in congenital heart disease genomics

Strong ferromagnetic metal-ligand exchange in a nickel bis(3,5-dipyridylverdazyl) complex

Combined Mutation Screening of NKX2-5, GATA4, and TBX5 in Congenital Heart Disease: Multiple Heterozygosity and Novel Mutations

Body composition and clinical outcome measures in patients with myotonic dystrophy type 1

Radical−Radical Interaction through a Saturated Link: Methylenebis-6-oxoverdazyl

Coordinated Hydrazone Ligands as Nucleophiles: Reactions of Fe(papy)2

Effect of deletion of the protein kinase PRKD1 on development of the mouse embryonic heart

Acetylation of TBX5 by KAT2B and KAT2A regulates heart and limb development

HDAC4 and 5 repression of TBX5 is relieved by protein kinase D1

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans

Zebrafish deficient for Muscleblind-like 2 exhibit features of myotonic dystrophy

Flies deficient in Muscleblind protein model features of myotonic dystrophy with altered splice forms of Z-band associated transcripts

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16

Coordination Chemistry of Verdazyl Radicals

Tropomyosin 1: Multiple roles in the developing heart and in the formation of congenital heart defects

High-content screening identifies small molecules that remove nuclear foci, affect MBNL distribution and CELF1 protein levels via a PKC-independent pathway in myotonic dystrophy cell lines

Verdazyl-ribose: A new radical for solid-state dynamic nuclear polarization at high magnetic field

Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot

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